Statistics for iMED ApS

4Total Devices

1Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Certificate health for iMED ApS

No certificates registered for this manufacturer.

Devices by risk class

Device catalog for iMED ApS

Showing 1–4 of 4 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
19-1000	`19-1000`	`05745000816019`	1	On the market
iMED Tooth Protector, double	`20-2000`	`05745000816026`	1	On the market
640012	`640012`	`05745000816002`	1	On the market
ME126607	`ME126607`	`05745000816033`	1	On the market

Device families (Basic UDI-DI) of iMED ApS

Showing 1–1 of 1 device families.

iMED Tooth Protector5745000816TPTPE7N

Market presence of iMED ApS

Devices placed in 1 country

Denmark4

EUDAMED update: Apr 8, 2026

iMED ApS

DK-MF-000032070

Active

Address: Skovdalsvej, 4 8300 Odder
Role: Manufacturer
Date of registration: Dec 21, 2022
Country: DK Denmark

About iMED ApS

SRN: DK-MF-000032070
Role: Manufacturer
Country: Denmark
Organization name: iMED ApS
EU VAT number: 29929777
EORI: DK29929777
Date of registration: Dec 21, 2022

Contact details for iMED ApS

Address: 4, SKOVDALSVEJ 8300 ODDER 8300 ODDER DENMARK
Phone: +45 2 999 82 22
Email: mail@i-MED.dk
Website: http://www.i-med.dk/

Validator

Name: Danish Medicines Agency, Pharmacovigilance & Medical Devices
SRN: DK-CA-042
Phone: +45 44 88 95 95
Email: dkma@dkma.dk

Officers and regulatory representatives of iMED ApS

THYSTRUP Frank
(a) the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; (b) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (c) the post-market surveillance obligations are complied with in accordance with Article 10(10); (d) the reporting obligations referred to in Articles 87 to 91 are fulfilled;
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